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Scientists have long toyed with the idea of putting to work a special class of biological catalysts, called ribozymes, as therapeutic agents. These molecular scissors would harness the activities of overly active genes that contribute to diseases like cancer by cutting their immediate products, messenger RNAs, into unusable pieces. The advantage of this approach, is that these molecules can be made to recognize very specific targets. This is reported in this month issue of EMBO reports.

Up until now, however, technical difficulties have hampered the development of such tools; the targets for these molecules are often folded extensively, making particular cleavage sites inaccessible to the catalyst. However, in the May 15 issue of EMBO reports, H. Kawasaki and K. Taira report on a technical breakthrough. By linking ribozymes to helicases, cellular components whose normal function is to smooth out folded RNAs to allow them to be translated into proteins, these investigators have managed to circumvent this folding difficulty. They have been able to efficiently inhibit the activities of a number of target RNAs, even at sites that are known to be inaccessible to regular ribozymes. This has further allowed them to develop a method for investigating the functions of random RNAs, creating a tool that may be invaluable in characterizing the functions of many of the previously unknown genes that have only recently been uncovered by various genome projects. Although we are not yet ready to treat any diseases using ribozymes, this study may indeed be a big step in the right direction.


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Contact: Ellen Peerenboom
ellen.peerenboom@embo.org
49-6221-8891-108
European Molecular Biology Laboratory
15-May-2002


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